19701-19-0 Usage
Uses
Used in Specialty Polymers Industry:
2-Vinylhexafluoroisopropanol is used as a monomer for the production of specialty polymers, which are known for their unique thermal, chemical, and electrical properties. Its incorporation into polymers enhances their performance in various applications, such as high-temperature resistance and chemical stability.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 2-Vinylhexafluoroisopropanol is utilized in the synthesis of fluorinated drugs. Its unique structure allows for the development of new pharmaceutical compounds with improved properties, such as enhanced bioavailability and targeted drug delivery.
Used in Agrochemical Industry:
2-Vinylhexafluoroisopropanol is employed in the synthesis of agrochemicals, including pesticides and herbicides. Its fluorinated nature contributes to the development of more effective and environmentally friendly agrochemicals.
Used in Surfactants Synthesis:
2-VINYLHEXAFLUOROISOPROPANOL is used as a key ingredient in the synthesis of specialized surfactants. The surfactants derived from 2-Vinylhexafluoroisopropanol exhibit unique properties, such as high surface activity and stability, making them suitable for various industrial applications, including coatings, adhesives, and detergents.
Used in Solvents Production:
2-Vinylhexafluoroisopropanol is utilized in the production of specialized solvents. These solvents offer unique properties, such as low toxicity, high boiling points, and excellent solubility, which make them ideal for use in various industrial processes, including chemical synthesis and material processing.
Used in Fluorinated Resins Synthesis:
In the field of materials science, 2-Vinylhexafluoroisopropanol is used in the synthesis of fluorinated resins. These resins possess exceptional properties, such as high thermal stability, chemical resistance, and low surface energy, making them suitable for applications in aerospace, automotive, and electronics industries.
Overall, 2-Vinylhexafluoroisopropanol's unique structure and properties make it a valuable compound in various industrial and research fields, including materials science, pharmaceuticals, and electronics. Its potential applications continue to expand as new discoveries and innovations are made in these areas.
Check Digit Verification of cas no
The CAS Registry Mumber 19701-19-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,7,0 and 1 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 19701-19:
(7*1)+(6*9)+(5*7)+(4*0)+(3*1)+(2*1)+(1*9)=110
110 % 10 = 0
So 19701-19-0 is a valid CAS Registry Number.
InChI:InChI=1/C5H4F6O/c1-2-3(12,4(6,7)8)5(9,10)11/h2,12H,1H2
19701-19-0Relevant academic research and scientific papers
Cheng, Jie-Fei,Huang, Yujin,Penuliar, Richard,Nishimoto, Masahiro,Liu, Larry,Arrhenius, Thomas,Yang, Guang,O'Leary, Eoin,Barbosa, Miguel,Barr, Rick,Dyck, Jason R. B.,Lopaschuk, Gary D.,Nadzan, Alex M.
, p. 4055 - 4058 (2006)
Discovery of 5-(1.1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-4,5- dihydroisoxazole-3-carboxamides as a new class of malonyl-coenzyme A decarboxylase (MCD) inhibitors is described. tert-Butyl 3-(5-(1,1,1.3,3,3- hexafluoro-2-hydroxypropan-2-yl)-4,5-dihydroi
Valerie, Martin,Molines, Huguette,Wakselman, Claude
, p. 139 - 142 (1995)
A two step synthesis of 1-bromo-4,4,4-trifluoro-3-(trifluoromethyl)but-2-ene in 35percent overall yield is reported starting from commercially available hexafluoroacetone.The electrophilic reactivity of this new compound towards various nucleophilic reage
